Compound Identification
SMILES
CCCCCCCCCCCCCCCC(=O)NCCCNP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O
InChIKey
InChIKey=MTNBAYQEOHERSG-JGJYTDKCSA-N
Formula
C212H282N82O117P20
Mass
6470.52
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleotides
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleotides
Subclass
Purine deoxyribonucleotides
Intermediate Tree Nodes
Purine deoxyribonucleoside bisphosphates
Direct Parent
Purine deoxyribonucleoside 3',5'-bisphosphates
Alternative Parents
Polysaccharide phosphates Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Purine 2'-deoxyribonucleoside monophosphates Ribonucleoside 3'-phosphates 6-aminopurines 6-oxopurines Hypoxanthines Aminopyrimidines and derivatives Dialkyl phosphates Pyrimidones Phosphoric monoester monoamides Hydropyrimidines Imidolactams N-acyl amines N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Amino acids and derivatives Lactams Ureas Secondary alcohols Secondary carboxylic acid amides Azacyclic compounds Oxacyclic compounds Primary amines Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Polysaccharide phosphate - Polysaccharide - Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Purine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Dialkyl phosphate - Phosphoric monoester monoamide - Organic phosphoric acid amide - Alkyl phosphate - Fatty amide - Pyrimidine - Imidolactam - Hydropyrimidine - Fatty acyl - N-acyl-amine - N-substituted imidazole - Phosphoric acid ester - Organic phosphoric acid derivative - Azole - Vinylogous amide - Imidazole - Heteroaromatic compound - Oxolane - Urea - Secondary carboxylic acid amide - Amino acid or derivatives - Secondary alcohol - Carboxamide group - Lactam - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Organic oxide - Organic oxygen compound - Alcohol - Carbonyl group - Amine - Hydrocarbon derivative - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine deoxyribonucleoside 3',5'-bisphosphates. These are purine ribobucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety, which lacks a hydroxyl group at position 2.
External Descriptors
Not available